Primary Device ID | 00848838091346 |
NIH Device Record Key | 9c8a5a26-b58f-4f3f-bfbc-351ade89c64c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | T3462-05-10 |
Company DUNS | 065769564 |
Company Name | REMEL, INC. |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |